Umbilical bleeding: a presenting feature for congenital afibrinogenemia
Umbilical bleeding: a presenting feature for congenital afibrinogenemia
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DOI：
10.1097/mbc.0000000000000368
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发表时间：
2015-10-01
影响因子：
1.1
通讯作者：
Shahverdi, Ehsan
中科院分区：
文献类型：
--
作者：
Abolghasemi, Hassan;Shahverdi, Ehsan
先天性无纤维蛋白原血症是一种非常罕见的遗传性凝血障碍，其特征是血浆纤维蛋白原（因子I）缺乏。世界文献中仅报道了约250例。我们描述了一例表现为脐带出血的先天性无纤维蛋白原血症病例。版权所有（c）2015威科集团。保留所有权利。
Congenital afibrinogenemia is a very rare inherited coagulation disorder characterized by absence of plasma fibrinogen (factor I). There are only about 250 cases reported in the world literature. We describe a case of congenital afibrinogenemia which presented as an umbilical cord bleeding. Copyright (c) 2015 Wolters Kluwer Health, Inc. All rights reserved.